Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_assertion> ?p ?o ?g. }
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- NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_assertion type Assertion NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_head.
- NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_assertion description "[One patient had compound heterozygous mutations in RDH5 and suffered from FAP with mild maculopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_provenance.
- NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_assertion evidence source_evidence_literature NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_provenance.
- NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_assertion SIO_000772 22559933 NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_provenance.
- NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_assertion wasDerivedFrom befree-20140225 NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_provenance.
- NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_assertion wasGeneratedBy ECO_0000203 NP363557.RAlupDL9gswwtPpjzCaYWP7_e7wAQWb4JnAu7GXskvQZM130_provenance.